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1.
J Pediatr Gastroenterol Nutr ; 76(2): e27-e35, 2023 02 01.
Artigo em Inglês | MEDLINE | ID: mdl-36705695

RESUMO

OBJECTIVES: Reports of prevalence of functional gastrointestinal disorders (FGIDs) in infants/toddlers are widely variable. Reasons for this variability are not yet fully understood. The objective of this study is to estimate the prevalence of FGIDs according to Rome IV criteria and to evaluate associated factors, in Italian infants and toddlers. METHODS: Subjects aged 0-48 months were enrolled by general pediatricians from 3 Italian regions. Parents or legal guardians were administered questionnaires including information about the child, the family, and GI symptoms according to Rome IV criteria. RESULTS: Five hundred eight infants aged 0-12 months [mean age 4.4 ± 3.4 months; females (F) 40.9%], and 268 children aged 13-48 months (mean age 30.8 ± 10.7 months; F 44.4%) were included. In infants, prevalence of FGIDs was 21.1%, and the most prevalent FGID was infant colic (9.3%). In toddlers, prevalence of FGIDs was 19.6%, with functional constipation being the most frequent disorder (16.1%). In infants, multivariable analysis found that being older, being the only child, and living in a rural environment were associated with a lower rate of FGIDs. Prevalence was, in contrast, higher in infants fed with formula. CONCLUSIONS: One out of 5 Italian infants and young children is affected by at least 1 FGID. The most frequent FGID in infants is infant colic, while in toddlers this is functional constipation. In infants, prevalence of FGIDs is lower if the subject has no siblings, and in children living in a rural environment, while formula feeding represents a risk factor for FGIDs occurrence.


Assuntos
Cólica , Gastroenteropatias , Feminino , Humanos , Lactente , Pré-Escolar , Estudos Transversais , Prevalência , Gastroenteropatias/epidemiologia , Gastroenteropatias/diagnóstico , Constipação Intestinal , Itália/epidemiologia , Fatores de Risco , Inquéritos e Questionários
2.
J Matern Fetal Neonatal Med ; 34(10): 1679-1682, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-31315488

RESUMO

PURPOSE: To evaluate the relation between CD34+ cells count in maternal blood and potential development of fetal congenital renal abnormalities. MATERIALS AND METHODS: We enrolled 16 women that gave birth to newborns carrying congenital renal malformations over a 3-year period and 48 women with uncomplicated pregnancies (controls) in a 1:3 ratio (three controls per case). RESULTS: CD34+ cells in the maternal peripheral blood were significantly lower in the group of women who gave birth to newborns carrying congenital renal malformations compared to the controls (p < .0001). CONCLUSIONS: CD34+ cells in maternal blood could be validated as a potential marker to predict the development of possible kidney malformations.


Assuntos
Anormalidades Congênitas , Feto , Estudos de Casos e Controles , Feminino , Sangue Fetal , Humanos , Recém-Nascido , Rim , Gravidez
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